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Transition From PBM to PBA Model: A Case Study in Innovative Contracting PBMI Drug Benefit Conference 2014 Craig Stern, PharmD, MBA, President Pro Pharma Pharmaceutical Consultants, Inc. February 4, 2014
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Transition From PBM to PBA Model: A Case Study in Innovative Contracting

PBMI Drug Benefit Conference 2014

Craig Stern, PharmD, MBA, President

Pro Pharma Pharmaceutical Consultants, Inc.

February 4, 2014

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GOALS

Determinative Pricing

Trend Variation Minimized

Cost Anchored to Manufacturer Price Inflation

Oversight of Cost with ability to make mid-term corrections

Oversight of Provider Performance

Allow for more Innovative Provider Performance standards

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PBA MODEL

PBA Responsibilities Claim Administration Network Management

Networks Custom Retail Custom Chain National Wrap

Fee Schedules Health Plan responsible for fees Custom MAC

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MODEL PARAMETERS

Cost Contraction based on “lesser of logic”

Elimination of “middle-man” incentives

Trend Management

PBA Administrative Services only arrangement

Ongoing Oversight

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TERM SHEET ELEMENTS Any multisource, branded generic, or OTC that is available from at least one generic

manufacturer will permit the member to pay generic co-pay

All drugs shall be dispensed as generic unless stipulated as DAW 1.

All drugs dispensed shall comply with the HP benefit design and formulary requirements

All claims will be priced according to “lesser of” logic on a per-claim basis.

“Lesser of” logic on a per-claim basis is based on the lesser of the AWP or WAC negotiated discount, the usual and customary as published by the pharmacy for non-membership patients, or the HP MAC. Dispensing fee will be added to the “lesser of” price.

The HP MAC is based on “lesser of” pricing including, but not limited to, the AWP or WAC negotiated discount, the State Medicaid MAC, the CMS FUL, or the usual and customary as published by the pharmacy for non-membership patients.

The HP MAC will be published on the web and updated monthly.

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TERM SHEET ELEMENTS

All claims shall contain valid and identifiable information including but not limited to: a) Member’s Identification including the Member number; b) valid NDC of the medication prescribed (that has not been termed by the

manufacturer or CMS); c) valid NPI or DEA for the prescribing physician as published by nationally

recognized databases; d) the package size of the medication dispensed; e) the quantity of the medication dispensed; f) estimated days’ supply; g) the correct DAW for Brand medications dispensed, if applicable; h) the strength of the medication dispensed.

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DEFINITIONS: SPECIFIC DESIRED ELEMENTS

AVERAGE WHOLESALE PRICE or (AWP) = WAC*1.2 and as set forth in the current price list in recognized sources such as Medi-Span, including its supplements, or other nationally recognized pricing source, including the Covered Manufacturer’s published AWP. However, if Medi-Span or the Covered Manufacture published AWP is in excess of the statutory definition, then PBM will be responsible for changing the published AWP to the post-settlement statutory AWP. The applicable AWP for prescriptions dispensed shall be based on the actual package-size submitted based on the 11 character NDC.

BRAND NAME DRUG means a brand name drug marketed under a proprietary, trademark-protected name (http://www.fda.gov/Drugs/default.htm).

CLEAN CLAIM is defined as an Rx not requiring any clarification from an MD and also includes complete and legible prescribing information from an actual doctor, for an eligible patient, actual valid pharmacy, and containing drug information such as valid and active NDC (Drug Name, Strength, Directions, MD Signature, and Quantity or Duration of Therapy).

GENERIC DRUG means a drug that is identical--or bioequivalent--to a brand name drug in dosage form, safety, strength, route of

administration, quality, performance characteristics and intended use. A generic drug is a medication approved by the FDA with an ANDA. An Abbreviated New Drug Application (ANDA) contains data that, when submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, provides for the review and ultimate approval of a generic drug product. (http://www.fda.gov/Drugs/default.htm).

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DEFINITIONS: SPECIFIC DESIRED ELEMENTS

MAXIMUM ALLOWABLE COST (MAC) means the maximum allowable cost of a drug pursuant to a list published by HP that establishes an upper limit reimbursement price for certain multiple-source drugs dispensed without regard to the specific manufacturer whose drug is dispensed. The MAC must be consistent with, and no more than, “the lesser of” the State Medicaid MAC, the CMS Federal Upper Limit (FUL), the Usual & Customary charge, or the contracted AWP discount on a per-drug basis.

NATIONAL PROVIDER IDENTIFIER (NPI) is a unique identification number issued by NCPDP for use by covered health care providers to identify Prescribers as required by the Health Insurance Portability and Accountability Act (HIPAA) Administrative Simplification Standard.

REQUIRED INFORMATION means complete, identifiable (and if submitted on paper, legible) Claim information required by the PBM contracted with the Health Plan. Required Information includes without limitation (a) Member’s identification number; (b) NDC of the medication prescribed; (c) the bottle size from which the medication is dispensed; (d) quantity of the medication dispensed; (e) estimated days supply of medication; (f) the correct DAW code for brand name medications; (g) an NPI number; (h) codes and cost information as designated by PBM for compound prescriptions; and (i) sales tax amounts.

WHOLESALE ACQUISITION COST (WAC) means a Pharmaceutical Company’s wholesale price for a drug provided by a Pharmaceutical Company to third-party pricing sources (e.g., Medi-Span) for inclusion in their price databases.

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CUSTOM MAC

Predicated on “Lesser of” Logic

Elements Include:

State Medicaid MAC

Federal Upper Limits (FUL)

Contracted AWP Discounts

ALL Generics Included

Pricing Updated Monthly

Published on Secure Website available to entire networks

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DIRECT CONTRACTING WITH CHAIN NETWORKS

Geo-Access Analysis

Identification of Major Players

Term Sheet for Negotiations

Custom MAC Vetting

Continuity of Rates Across the Networks

Restricted Network Acceptable if necessary

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DIRECT PROVIDER CONTRACTING

PROS

Direct Contracting Preferable to Chains

Transparency in All Pricing

CONS

Network Management / Oversight

MAC Fixed Fees vs. GER

Restricted Network / Restricted Access

Local vs. National Contracting

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OVERSIGHT & MANAGEMENT OF THE PBA MODEL

Review of Plan Design Worksheets to ensure claim adjudication logic consistent with benefit logic

Screening of Invoices

Accounts Payable reviews at every invoice

MAC Updates Monthly and more frequently for access issues

Monthly Financial and Clinical Performance Reviews

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Pro Pharma

Pharmaceutical Consultants, Inc.

P.O. Box 280130

Northridge, CA 91328-0130

(818) 701-5438

(818) 701 – 0249 Fax

Email: [email protected]

…or Visit Our Website at:

www.propharmaconsultants.com Also find us on…


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